Results 71 to 80 of about 41,087 (216)

Antinuclear antibodies in COVID 19

open access: yesClinical and Translational Science, 2021
Paolo Muratori   +3 more
doaj   +1 more source

Gastrointestinal strictures in a pediatric patient with Satoyoshi syndrome

open access: yesJPGN Reports, EarlyView.
Abstract We present a novel case of gastrointestinal strictures in a young girl with Satoyoshi syndrome (SS), highlighting multi‐system features of alopecia universalis, painful muscle cramps with dystonia, aberrant growth velocity, and skeletal abnormalities.
Katherine (Tusia) Pohoreski   +5 more
wiley   +1 more source

Hepatopulmonary syndrome as presentation of pediatric metabolic dysfunction‐associated steatohepatitis

open access: yesJPGN Reports, EarlyView.
Abstract Childhood obesity is rising and leading to serious co‐morbidities, among which is metabolic dysfunction‐associated steatotic liver disease (MASLD) predisposing individuals to cirrhosis. We describe a young 11‐year‐old Hispanic male who presented with hepatopulmonary syndrome secondary to cirrhotic portal hypertension from metabolic dysfunction‐
Shruti Sakhuja   +6 more
wiley   +1 more source

Detection of Antinuclear Antibodies in HIV-Infected Individuals

open access: yesJournal of Associated Medical Sciences, 2017
Background: The causes of autoimmune diseases (ADs) are still not clearly known, but it is believed that diseases are propelled by multiple factors including genetic, hormone and environmental factors.
Kanyanee Promsawan   +10 more
doaj  

Conjoint glutamic acid decarboxylase 65 and P/Q voltage gated calcium channel antibodies in autoimmune epilepsy: A case report

open access: yesEpilepsy and Behavior Case Reports, 2018
Numerous autoantibodies are implicated in the pathogenesis of autoimmune epilepsy. In the past decade, many case series reported the association of glutamic acid decarboxylase 65 (GAD 65) antibodies with epilepsy.
Mohamed AlKhaja   +3 more
doaj   +1 more source

Itching for a diagnosis: Dysesthesias as an atypical presentation of Wilson disease in an adolescent—Case report

open access: yesJPGN Reports, EarlyView.
Abstract Wilson disease (WD) is an autosomal recessive disorder of hepatic copper metabolism with varied clinical presentations. We describe a 15‐year‐old male referred for elevated aminotransferases, burning facial pruritis, scalp dysesthesias, and chronic bilateral lower extremity edema.
Tierra L. R. Mosher   +2 more
wiley   +1 more source

Determinación de anticuerpos antinucleares en la anemia hemolítica autoinmune y la púrpura trombocitopénica autoinmune Determination of antinuclear antibodies in autoimmune hemolytic anemia and autoimmune thrombocytopenic purpura

open access: yesRevista Cubana de Hematología, Inmunología y Hemoterapia, 2002
Se detectó la presencia de anticuerpos antinucleares mediante un método de inmunofluorescencia indirecta en uno de los 18 pacientes estudiados con anemia hemolítica autoinmune y en 3 de los 16 pacientes con púrpura trombocitopénica autoinmune.
Ana M Guerreiro Hernández   +6 more
doaj  

Long‐Term Dermoscopic Evolution of Reticular Erythematous Mucinosis: Case Report

open access: yesJEADV Clinical Practice, EarlyView.
ABSTRACT Reticular erythematous mucinosis is a rare dermatosis with a challenging diagnosis. To date, its dermoscopic features have not been well characterised in the literature. Only a limited number of case reports have described dermoscopic findings that may be indicative of the disorder, including the presence of dotted and linear vessels, as well ...
Grażyna Kamińska‐Winciorek   +4 more
wiley   +1 more source

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